E827 Full

FROM THE AMERICAN ACADEMY OF PEDIATRICS
Organizational Principles to Guide and Dene the Child

Health Care System and/or Improve the Health of all Children
POLICY STATEMENT
Breastfeeding and the Use of Human Milk

SECTION ON BREASTFEEDING
KEY WORDS
breastfeeding, complementary foods, infant nutrition, lactation,
human milk, nursing
ABBREVIATIONS
AAPAmerican Academy of Pediatrics
AHRQAgency for Healthcare Research and Quality
CDCCenters for Disease Control and Prevention
CIcondence interval
CMVcytomegalovirus
DHAdocosahexaenoic acid
NECnecrotizing enterocolitis
ORodds ratio
SIDSsudden infant death syndrome
WHOWorld Health Organization
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Academy of Pediatrics and its Board of Directors. All authors
have led conict of interest statements with the American
Academy of Pediatrics. Any conicts have been resolved through
a process approved by the Board of Directors. The American
Academy of Pediatrics has neither solicited nor accepted any
commercial involvement in the development of the content of
this publication.
All policy statements from the American Academy of Pediatrics
automatically expire 5 years after publication unless reafrmed,
revised, or retired at or before that time.
abstract
Breastfeeding and human milk are the normative standards for infant
feeding and nutrition. Given the documented short- and long-term medical and neurodevelopmental advantages of breastfeeding, infant nutrition should be considered a public health issue and not only
a lifestyle choice. The American Academy of Pediatrics reafrms its
recommendation of exclusive breastfeeding for about 6 months, followed by continued breastfeeding as complementary foods are introduced, with continuation of breastfeeding for 1 year or longer as
mutually desired by mother and infant. Medical contraindications to
breastfeeding are rare. Infant growth should be monitored with the
World Health Organization (WHO) Growth Curve Standards to avoid mislabeling infants as underweight or failing to thrive. Hospital routines
to encourage and support the initiation and sustaining of exclusive breastfeeding should be based on the American Academy of
Pediatrics-endorsed WHO/UNICEF Ten Steps to Successful Breastfeeding. National strategies supported by the US Surgeon Generals Call
to Action, the Centers for Disease Control and Prevention, and The
Joint Commission are involved to facilitate breastfeeding practices in
US hospitals and communities. Pediatricians play a critical role in
their practices and communities as advocates of breastfeeding and
thus should be knowledgeable about the health risks of not breastfeeding, the economic benets to society of breastfeeding, and the
techniques for managing and supporting the breastfeeding dyad. The
Business Case for Breastfeeding details how mothers can maintain
lactation in the workplace and the benets to employers who facilitate this practice. Pediatrics 2012;129:e827e841
INTRODUCTION
www.pediatrics.org/cgi/doi/10.1542/peds.2011-3552
doi:10.1542/peds.2011-3552
PEDIATRICS (ISSN Numbers: Print, 0031-4005; Online, 1098-4275).
Copyright 2012 by the American Academy of Pediatrics
PEDIATRICS Volume 129, Number 3, March 2012
Six years have transpired since publication of the last policy statement
of the American Academy of Pediatrics (AAP) regarding breastfeeding.1
Recently published research and systematic reviews have reinforced
the conclusion that breastfeeding and human milk are the reference
normative standards for infant feeding and nutrition. The current
statement updates the evidence for this conclusion and serves as
a basis for AAP publications that detail breastfeeding management
and infant nutrition, including the AAP Breastfeeding Handbook for
Physicians,2 AAP Sample Hospital Breastfeeding Policy for Newborns,3
AAP Breastfeeding Residency Curriculum,4 and the AAP Safe and
Healthy Beginnings Toolkit.5 The AAP reafrms its recommendation
of exclusive breastfeeding for about 6 months, followed by continued
breastfeeding as complementary foods are introduced, with continuation
e827
of breastfeeding for 1 year or longer

as mutually desired by mother and
infant.
EPIDEMIOLOGY
Information regarding breastfeeding
rates and practices in the United States
is available from a variety of government data sets, including the Centers
for Disease Control and Prevention (CDC)
National Immunization Survey,6 the
NHANES,7 and Maternity Practices and
Infant Nutrition and Care.8 Drawing on
these data and others, the CDC has
published the Breastfeeding Report
Card, which highlights the degree of
progress in achieving the breastfeeding goals of the Healthy People 2010
targets as well as the 2020 targets
(Table 1).911
The rate of initiation of breastfeeding
for the total US population based on
the latest National Immunization Survey data are 75%.11 This overall rate,
however, obscures clinically signicant sociodemographic and cultural
differences. For example, the breastfeeding initiation rate for the Hispanic
or Latino population was 80.6%, but
for the non-Hispanic black or African
American population, it was 58.1%.
Among low-income mothers (participants in the Special Supplemental
Nutrition Program for Women, Infants,
and Children [WIC]), the breastfeeding
initiation rate was 67.5%, but in those
TABLE 1 Healthy People Targets 2010 and

2020(%)
2007a
Any breastfeeding
Ever
6 mo
1y
Exclusive breastfeeding
To 3 mo
To 6 mo
Worksite lactation support
Formula use in rst 2 d
a
2010 2020
Target Target
75.0
43.8
22.4
75
50
25
81.9
60.5
34.1
33.5
13.8
25
25.6
40
17
44.3
23.7
38.0
15.6
2007 data reported in 2011.10
e828
with a higher income ineligible for

WIC, it was 84.6%.12 Breastfeeding
initiation rate was 37% for low-income
non-Hispanic black mothers.7 Similar
disparities are age-related; mothers
younger than 20 years initiated breastfeeding at a rate of 59.7% compared
with the rate of 79.3% in mothers
older than 30 years. The lowest rates
of initiation were seen among nonHispanic black mothers younger than
20 years, in whom the breastfeeding
initiation rate was 30%.7
Although over the past decade, there
has been a modest increase in the rate
of any breastfeeding at 3 and 6
months, in none of the subgroups
have the Healthy People 2010 targets
been reached. For example, the 6month any breastfeeding rate for
the total US population was 43%, the
rate for the Hispanic or Latino subgroup was 46%, and the rate for the
non-Hispanic black or African American subgroup was only 27.5%. Rates
of exclusive breastfeeding are further
from Healthy People 2010 targets, with
only 13% of the US population meeting
the recommendation to breastfeed exclusively for 6 months. Thus, it appears
that although the breastfeeding initiation rates have approached the
2010 Healthy People targets, the targets for duration of any breastfeeding
and exclusive breastfeeding have not
been met.
Furthermore, 24% of maternity services provide supplements of commercial infant formula as a general
practice in the rst 48 hours after
birth. These observations have led to
the conclusion that the disparities in
breastfeeding rates are also associated with variations in hospital routines, independent of the populations
served. As such, it is clear that greater
emphasis needs to be placed on improving and standardizing hospitalbased practices to realize the newer
2020 targets (Table 1).
INFANT OUTCOMES
Methodologic Issues
Breastfeeding results in improved infant and maternal health outcomes in
both the industrialized and developing
world. Major methodologic issues have
been raised as to the quality of some
of these studies, especially as to the
size of the study populations, quality of
the data set, inadequate adjustment
for confounders, absence of distinguishing between any or exclusive
breastfeeding, and lack of a dened
causal relationship between breastfeeding and the specic outcome. In
addition, there are inherent practical
and ethical issues that have precluded
prospective randomized interventional
trials of different feeding regimens.
As such, the majority of published
reports are observational cohort
studies and systematic reviews/metaanalyses.
To date, the most comprehensive
publication that reviews and analyzes
the published scientic literature that
compares breastfeeding and commercial infant formula feeding as to
health outcomes is the report prepared by the Evidence-based Practice
Centers of the Agency for Healthcare
Research and Quality (AHRQ) of the US
Department of Health Human Services
titled Breastfeeding and Maternal and
Infant Health Outcomes in Developed
Countries.13 The following sections
summarize and update the AHRQ metaanalyses and provide an expanded
analysis regarding health outcomes.
Table 2 summarizes the dose-response
relationship between the duration of
breastfeeding and its protective effect.
Respiratory Tract Infections and
Otitis Media
The risk of hospitalization for lower
respiratory tract infections in the rst
year is reduced 72% if infants breastfed
exclusively for more than 4 months.13,14
Infants who exclusively breastfed for 4
TABLE 2 Dose-Response Benets of Breastfeedinga

Condition
% Lower Riskb
Otitis media13
Otitis media13
Recurrent otitis media15
23
50
77
Upper respiratory
tract infection17
Lower respiratory
tract infection13
Lower respiratory
tract infection15
Asthma13
Asthma13
Breastfeeding
Comments
ORc
95% CI
Exclusive BF
Compared with
BF 4 to <6 mod
Exclusive BF
0.77
0.50
1.95
0.640.91
0.360.70
1.063.59
63
Any
3 or 6 mo
Exclusive BF
6 mod
>6 mo
0.30
0.180.74
72
4 mo
Exclusive BF
0.28
0.140.54
77
1.2714.35
0.60
0.74
0.430.82
0.60.92
RSV bronchiolitis16
NEC19
74
77
>4 mo
NICU stay
0.26
0.23
0.0740.9
0.510.94
Atopic dermatitis27
27
>3 mo
0.84
0.591.19
Atopic dermatitis27
42
>3 mo
0.58
0.410.92
Gastroenteritis13,14
Inammatory bowel
disease32
Obesity13
Celiac disease31
64
31
Any
Any
Compared with
BF 4 to <6 mod
Atopic family history
No atopic family
history
Preterm infants
Exclusive HM
Exclusive BFnegative
family history
Exclusive BFpositive
family history
4.27
40
26
Exclusive BF
6 mod
3 mo
3 mo
0.36
0.69
0.320.40
0.510.94
24
52
Any
>2 mo
0.76
0.48
0.670.86
0.400.89
Type 1 diabetes13,42
Type 2 diabetes13,43
Leukemia (ALL)13,46
Leukemia (AML)13,45
SIDS13
30
40
20
15
36
>3 mo
Any
>6 mo
>6 mo
Any >1 mo
0.71
0.61
0.80
0.85
0.64
0.540.93
0.440.85
0.710.91
0.730.98
0.570.81
Gluten exposure
when BF
Exclusive BF
ALL, acute lymphocytic leukemia; AML, acute myelogenous leukemia; BF, breastfeeding; HM, human milk; RSV, respiratory
syncytial virus.
a
Pooled data.
b
% lower risk refers to lower risk while BF compared with feeding commercial infant formula or referent group
specied.
c
OR expressed as increase risk for commercial formula feeding.
d
Referent group is exclusive BF 6 months.
to 6 months had a fourfold increase

in the risk of pneumonia compared
with infants who exclusively breastfed
for more than 6 months.15 The severity
(duration of hospitalization and oxygen
requirements) of respiratory syncytial
virus bronchiolitis is reduced by 74%
in infants who breastfed exclusively for
4 months compared with infants who
never or only partially breastfed.16
infants who exclusively breastfed for 6

months.17
Any breastfeeding compared with exclusive commercial infant formula

feeding will reduce the incidence of
otitis media (OM) by 23%.13 Exclusive
breastfeeding for more than 3 months
reduces the risk of otitis media by
50%. Serious colds and ear and throat
infections were reduced by 63% in
Necrotizing Enterocolitis
Gastrointestinal Tract Infections

Any breastfeeding is associated with
a 64% reduction in the incidence of
nonspecic gastrointestinal tract infections, and this effect lasts for 2 months
after cessation of breastfeeding.13,14,17,18
Meta-analyses of 4 randomized clinical

trials performed over the period 1983
to 2005 support the conclusion that
feeding preterm infants human milk is
associated with a signicant reduction
(58%) in the incidence of necrotizing
enterocolitis (NEC).13 A more recent
study of preterm infants fed an exclusive human milk diet compared with
those fed human milk supplemented
with cow-milk-based infant formula products noted a 77% reduction in NEC.19
One case of NEC could be prevented if
10 infants received an exclusive human
milk diet, and 1 case of NEC requiring
surgery or resulting in death could be
prevented if 8 infants received an exclusive human milk diet.19
Sudden Infant Death Syndrome
and Infant Mortality
Meta-analyses with a clear denition of
degree of breastfeeding and adjusted
for confounders and other known risks
for sudden infant death syndrome
(SIDS) note that breastfeeding is associated with a 36% reduced risk of
SIDS.13 Latest data comparing any versus exclusive breastfeeding reveal that
for any breastfeeding, the multivariate
odds ratio (OR) is 0.55 (95% condence
interval [CI], 0.440.69). When computed for exclusive breastfeeding, the
OR is 0.27 (95% CI, 0.270.31).20 A proportion (21%) of the US infant mortality
has been attributed, in part, to the increased rate of SIDS in infants who
were never breastfed.21 That the positive effect of breastfeeding on SIDS
rates is independent of sleep position
was conrmed in a large case-control
study of supine-sleeping infants.22,23
It has been calculated that more than
900 infant lives per year may be saved
in the United States if 90% of mothers
exclusively breastfed for 6 months.24 In
the 42 developing countries in which
90% of the worlds childhood deaths occur, exclusive breastfeeding for 6 months
and weaning after 1 year is the most
effective intervention, with the potential
of preventing more than 1 million infant
deaths per year, equal to preventing 13%
of the worlds childhood mortality.25
Allergic Disease
There is a protective effect of exclusive
breastfeeding for 3 to 4 months in
e829
reducing the incidence of clinical

asthma, atopic dermatitis, and eczema
by 27% in a low-risk population and
up to 42% in infants with positive
family history.13,26 There are conicting studies that examine the timing of
adding complementary foods after 4
months and the risk of allergy, including
food allergies, atopic dermatitis, and
asthma, in either the allergy-prone or
nonatopic individual.26 Similarly, there
are no convincing data that delaying
introduction of potentially allergenic
foods after 6 months has any protective
effect.2730 One problem in analyzing
this research is the low prevalence of
exclusive breastfeeding at 6 months in
the study populations. Thus, research
outcomes in studies that examine the
development of atopy and the timing of
introducing solid foods in partially
breastfed infants may not be applicable to exclusively breastfed infants.
Celiac Disease
There is a reduction of 52% in the risk
of developing celiac disease in infants
who were breastfed at the time of
gluten exposure.31 Overall, there is an
association between increased duration of breastfeeding and reduced risk
of celiac disease when measured as
the presence of celiac antibodies. The
critical protective factor appears to
be not the timing of the gluten exposure but the overlap of breastfeeding
at the time of the initial gluten ingestion. Thus, gluten-containing foods
should be introduced while the infant
is receiving only breast milk and not
infant formula or other bovine milk
products.
Inammatory Bowel Disease
Breastfeeding is associated with a
31% reduction in the risk of childhood inammatory bowel disease.32
The protective effect is hypothesized
to result from the interaction of the
immunomodulating effect of human
milk and the underlying genetic
e830
susceptibility of the infant. Different

patterns of intestinal colonization in
breastfed versus commercial infant
formulafed infants may add to the
preventive effect of human milk.33
Obesity
Because rates of obesity are signicantly lower in breastfed infants, national campaigns to prevent obesity
begin with breastfeeding support.34,35
Although complex factors confound
studies of obesity, there is a 15% to
30% reduction in adolescent and adult
obesity rates if any breastfeeding occurred in infancy compared with no
breastfeeding.13,36 The Framingham
Offspring study noted a relationship of
breastfeeding and a lower BMI and
higher high-density lipoprotein concentration in adults.37 A sibling difference model study noted that the
breastfed sibling weighed 14 pounds
less than the sibling fed commercial
infant formula and was less likely to
reach BMI obesity threshold.38 The
duration of breastfeeding also is inversely related to the risk of overweight; each month of breastfeeding
being associated with a 4% reduction
in risk.14
The interpretation of these data is
confounded by the lack of a denition
in many studies of whether human
milk was given by breastfeeding or by
bottle. This is of particular importance,
because breastfed infants self-regulate
intake volume irrespective of maneuvers that increase available milk volume, and the early programming of
self-regulation, in turn, affects adult
weight gain.39 This concept is further
supported by the observations that
infants who are fed by bottle, formula,
or expressed breast milk will have
increased bottle emptying, poorer selfregulation, and excessive weight gain
in late infancy (older than 6 months)
compared with infants who only nurse
from the breast.40,41
Diabetes
Up to a 30% reduction in the incidence
of type 1 diabetes mellitus is reported
for infants who exclusively breastfed for
at least 3 months, thus avoiding exposure to cow milk protein.13,42 It has been
postulated that the putative mechanism
in the development of type 1 diabetes
mellitus is the infants exposure to cow
milk -lactoglobulin, which stimulates
an immune-mediated process crossreacting with pancreatic cells. A reduction of 40% in the incidence of type
2 diabetes mellitus is reported, possibly reecting the long-term positive
effect of breastfeeding on weight control and feeding self-regulation.43
Childhood Leukemia and
Lymphoma
There is a reduction in leukemia
that is correlated with the duration of
breastfeeding.14,44 A reduction of 20%
in the risk of acute lymphocytic leukemia and 15% in the risk of acute myeloid leukemia in infants breastfed for
6 months or longer.45,46 Breastfeeding
for less than 6 months is protective but
of less magnitude (approximately 12%
and 10%, respectively). The question of
whether the protective effect of breastfeeding is a direct mechanism of human
milk on malignancies or secondarily
mediated by its reduction of early childhood infections has yet to be answered.
Neurodevelopmental Outcomes
Consistent differences in neurodevelopmental outcome between breastfed
and commercial infant formulafed
infants have been reported, but the
outcomes are confounded by differences
in parental education, intelligence, home
environment, and socioeconomic status.13,47 The large, randomized Promotion of Breastfeeding Intervention
Trial provided evidence that adjusted
outcomes of intelligence scores and
teachers ratings are signicantly
greater in breastfed infants.4850 In
addition, higher intelligence scores

are noted in infants who exclusively
breastfed for 3 months or longer, and
higher teacher ratings were observed
if exclusive breastfeeding was practiced
for 3 months or longer. Signicantly
positive effects of human milk feeding
on long-term neurodevelopment are observed in preterm infants, the population more at risk for these adverse
neurodevelopmental outcomes.5154
PRETERM INFANTS
There are several signicant shortand long-term benecial effects of
feeding preterm infants human milk.
Lower rates of sepsis and NEC indicate
that human milk contributes to the
development of the preterm infants
immature host defense.19,5559 The benets of feeding human milk to preterm
infants are realized not only in the NICU
but also in the fewer hospital readmissions for illness in the year after
NICU discharge.51,52 Furthermore, the
implications for a reduction in incidence of NEC include not only lower
mortality rates but also lower long-term
growth failure and neurodevelopmental
disabilities.60,61 Clinical feeding tolerance is improved, and the attainment of
full enteral feeding is hastened by a diet
of human milk.51,52,59
Neurodevelopmental outcomes are improved by the feeding of human milk.
Long-term studies at 8 years of age
through adolescence suggest that intelligence test results and white matter
and total brain volumes are greater in
subjects who had received human milk
as infants in the NICU.53,54 Extremely
preterm infants receiving the greatest
proportion of human milk in the NICU
had signicantly greater scores for
mental, motor, and behavior ratings at
ages 18 months and 30 months.51,52
These data remain signicant after
adjustment for confounding factors,
such as maternal age, education, marital status, race, and infant morbidities.
These neurodevelopmental outcomes

are associated with predominant and
not necessarily exclusive human milk
feeding. Human milk feeding in the NICU
also is associated with lower rates of
severe retinopathy of prematurity.62,63
Long-term studies of preterm infants
also suggest that human milk feeding
is associated with lower rates of metabolic syndrome, and in adolescents, it
is associated with lower blood pressures and low-density lipoprotein concentrations and improved leptin and
insulin metabolism.64,65
The potent benets of human milk are
such that all preterm infants should
receive human milk (Table 3). Mothers
own milk, fresh or frozen, should be
the primary diet, and it should be
fortied appropriately for the infant
born weighing less than 1.5 kg. If
mothers own milk is unavailable despite signicant lactation support, pasteurized donor milk should be used.19,66
Quality control of pasteurized donor
milk is important and should be monitored. New data suggest that mothers
own milk can be stored at refrigerator
temperature (4C) in the NICU for as
long as 96 hours.67 Data on thawing,
warming, and prolonged storage need
updating. Practices should involve protocols that prevent misadministration
of milk.
MATERNAL OUTCOMES
Both short- and long-term health benets accrue to mothers who breastfeed. Such mothers have decreased
postpartum blood loss and more rapid
involution of the uterus. Continued
breastfeeding leads to increased child
spacing secondary to lactational amenorrhea. Prospective cohort studies
have noted an increase in postpartum
depression in mothers who do not
breastfeed or who wean early. 68 A
large prospective study on child abuse
and neglect perpetuated by mothers
found, after correcting for potential
TABLE 3 Recommendations on
Breastfeeding Management for
Preterm Infants
1. All preterm infants should receive human milk.
Human milk should be fortied, with protein,
minerals, and vitamins to ensure optimal
nutrient intake for infants weighing <1500 g
at birth.
Pasteurized donor human milk, appropriately
fortied, should be used if mothers own milk
is unavailable or its use is contraindicated.
2. Methods and training protocols for manual and
mechanical milk expression must be available
to mothers.
3. Neonatal intensive care units should possess
evidence-based protocols for collection,
storage, and labeling of human milk.150
4. Neonatal intensive care units should prevent the
misadministration of human milk (http://www.
cdc.gov/breastfeeding/recommendations/
other_mothers_milk.htm).
5. There are no data to support routinely culturing
human milk for bacterial or other organisms.151
confounders, that the rate of abuse/

neglect was signicantly increased for
mothers who did not breastfeed as
opposed to those who did (OR: 2.6;
95% CI: 1.73.9).69
Studies of the overall effect of breastfeeding on the return of the mothers
to their pre-pregnancy weight are inconclusive, given the large numbers of
confounding factors on weight loss
(diet, activity, baseline BMI, ethnicity).13
In a covariate-adjusted study of more
than 14 000 women postpartum, mothers who exclusively breastfed for longer than 6 months weighed 1.38 kg less
than those who did not breastfeed.70
In mothers without a history of gestational diabetes, breastfeeding duration
was associated with a decreased risk
of type 2 diabetes mellitus; for each
year of breastfeeding, there was a decreased risk of 4% to 12%.71,72 No benecial effect for breastfeeding was
noted in mothers who were diagnosed
with gestational diabetes.
The longitudinal Nurses Health Study
noted an inverse relationship between
the cumulative lifetime duration of
breastfeeding and the development of
rheumatoid arthritis.73 If cumulative
duration of breastfeeding exceeded 12
e831
months, the relative risk of rheumatoid arthritis was 0.8 (95% CI: 0.81.0),
and if the cumulative duration of
breastfeeding was longer than 24
months, the relative risk of rheumatoid arthritis was 0.5 (95% CI:
0.30.8).73 An association between
cumulative lactation experience and
the incidence of adult cardiovascular
disease was reported by the Womens
Health Initiative in a longitudinal study
of more than 139 000 postmenopausal
women.74 Women with a cumulative
lactation history of 12 to 23 months
had a signicant reduction in hypertension (OR: 0.89; 95% CI: 0.840.93),
hyperlipidemia (OR: 0.81; 95% CI: 0.76
0.87), cardiovascular disease (OR:
0.90; 95% CI: 0.850.96), and diabetes
(OR: 0.74; 95% CI: 0.650.84).
DURATION OF EXCLUSIVE
BREASTFEEDING
Cumulative lactation experience also

correlates with a reduction in both
breast (primarily premenopausal) and
ovarian cancer.13,14,75 Cumulative duration of breastfeeding of longer than
12 months is associated with a 28%
decrease in breast cancer (OR: 0.72;
95% CI: 0.650.8) and ovarian cancer
(OR: 0.72; 95% CI: 0.540.97).76 Each
year of breastfeeding has been calculated to result in a 4.3% reduction in
breast cancer.76,77
Compared with infants who never

breastfed, infants who were exclusively breastfed for 4 months had
signicantly greater incidence of lower
respiratory tract illnesses, otitis media, and diarrheal disease than infants
exclusively breastfed for 6 months or
longer.15,18 When compared with infants who exclusively breastfed for longer than 6 months, those exclusively
breastfed for 4 to 6 months had a fourfold increase in the risk of pneumonia.15
Furthermore, exclusively breastfeeding
for 6 months extends the period of
lactational amenorrhea and thus improves child spacing, which reduces
the risk of birth of a preterm infant.81
ECONOMIC BENEFITS
A detailed pediatric cost analysis
based on the AHRQ report concluded
that if 90% of US mothers would comply
with the recommendation to breastfeed
exclusively for 6 months, there would be
a savings of $13 billion per year.24 The
savings do not include those related to
a reduction in parental absenteeism
from work or adult deaths from diseases acquired in childhood, such as
asthma, type 1 diabetes mellitus, or
obesity-related conditions. Strategies
that increase the number of mothers
who breastfeed exclusively for about
6 months would be of great economic
benet on a national level.
e832
The AAP recommends exclusive breastfeeding for about 6 months, with continuation of breastfeeding for 1 year or
longer as mutually desired by mother
and infant, a recommendation concurred to by the WHO78 and the Institute of Medicine.79
Support for this recommendation of
exclusive breastfeeding is found in the
differences in health outcomes of infants breastfed exclusively for 4 vs 6
months, for gastrointestinal disease,
otitis media, respiratory illnesses,
and atopic disease, as well as differences in maternal outcomes of
delayed menses and postpartum
weight loss.15,18,80
The AAP is cognizant that for some

infants, because of family and medical
history, individual developmental status,
and/or social and cultural dynamics,
complementary feeding, including glutencontaining grains, begins earlier than
6 months of age.82,83 Because breastfeeding is immunoprotective, when such
complementary foods are introduced, it
is advised that this be done while the
infant is feeding only breastmilk.82
Mothers should be encouraged to continue breastfeeding through the rst
year and beyond as more and varied

complementary foods are introduced.
CONTRAINDICATIONS TO
BREASTFEEDING
There are a limited number of medical
conditions in which breastfeeding is
contraindicated, including an infant with
the metabolic disorder of classic galactosemia. Alternating breastfeeding
with special protein-free or modied
formulas can be used in feeding infants with other metabolic diseases
(such as phenylketonuria), provided
that appropriate blood monitoring is
available. Mothers who are positive for
human T-cell lymphotrophic virus type
I or II84 or untreated brucellosis85
should not breastfeed nor provide expressed milk to their infants Breastfeeding should not occur if the mother
has active (infectious) untreated tuberculosis or has active herpes simplex lesions on her breast; however,
expressed milk can be used because
there is no concern about these infectious organisms passing through
the milk. Breastfeeding can be resumed when a mother with tuberculosis is treated for a minimum of 2
weeks and is documented that she is
no longer infectious.86 Mothers who
develop varicella 5 days before through
2 days after delivery should be separated from their infants, but their
expressed milk can be used for feeding.87 In 2009, the CDC recommended
that mothers acutely infected with
H1N1 inuenza should temporarily be
isolated from their infants until they
are afebrile, but they can provide
expressed milk for feeding.88
In the industrialized world, it is not recommended that HIV-positive mothers
breastfeed. However, in the developing
world, where mortality is increased in
non-breastfeeding infants from a combination of malnutrition and infectious
diseases, breastfeeding may outweigh
the risk of the acquiring HIV infection
from human milk. Infants in areas

with endemic HIV who are exclusively
breastfed for the rst 3 months are at
a lower risk of acquiring HIV infection
than are those who received a mixed
diet of human milk and other foods
and/or commercial infant formula.89
Recent studies document that combining exclusive breastfeeding for 6
months with 6 months of antiretroviral
therapy signicantly decreases the
postnatal acquisition of HIV-1.90,91
There is no contraindication to breastfeeding for a full-term infant whose
mother is seropositive for cytomegalovirus (CMV). There is a possibility
that CMV acquired from mothers milk
may be associated with a late-onset
sepsis-like syndrome in the extremely
low birth weight (birth weight <1500
g) preterm infant. Although not associated with long-term abnormalities,
such a syndrome may warrant antiviral therapy.92 The value of routinely
feeding human milk from seropositive
mothers to preterm infants outweighs
the risks of clinical disease, especially
because no long-term neurodevelopmental abnormalities have been reported.93 Freezing of milk reduces but
does not eliminate CMV.94 Heating, either as Holder pasteurization (heating
at 62.5C for 30 minutes) or hightemperature short pasteurization
(72C for 510 seconds) eliminates
the viral load from the milk but also
affects bioactive factors and nutrients.95
Thus, fresh mothers own milk is preferable for routinely feeding all preterm
infants.
Maternal substance abuse is not a
categorical contraindication to breastfeeding. Adequately nourished narcoticdependent mothers can be encouraged
to breastfeed if they are enrolled in
a supervised methadone maintenance
program and have negative screening
for HIV and illicit drugs.96 Street drugs
such as PCP (phencyclidine), cocaine,
and cannabis can be detected in human
milk, and their use by breastfeeding

mothers is of concern, particularly
with regard to the infants long-term
neurobehavioral development and thus
are contraindicated.97 Alcohol is not
a galactogogue; it may blunt prolactin
response to suckling and negatively
affects infant motor development.98,99
Thus, ingestion of alcoholic beverages
should be minimized and limited to an
occasional intake but no more than
0.5 g alcohol per kg body weight,
which for a 60 kg mother is approximately 2 oz liquor, 8 oz wine, or 2
beers.100 Nursing should take place
2 hours or longer after the alcohol
intake to minimize its concentration in
the ingested milk.101 Maternal smoking is not an absolute contraindication to breastfeeding but should be
strongly discouraged, because it is associated with an increased incidence
in infant respiratory allergy102 and
SIDS.103 Smoking should not occur in
the presence of the infant so as to
minimize the negative effect of secondary passive smoke inhalation.104
Smoking is also a risk factor for low
milk supply and poor weight gain.105,106
MATERNAL DIET
Well-nourished lactating mothers have
an increased daily energy need of 450
to 500 kcal/day that can be met by a
modest increase in a normally balanced
varied diet.107109 Although dietary reference intakes for breastfeeding mothers are similar to or greater than those
during pregnancy, there is no routine
recommendation for maternal supplements during lactation.108,109,110 Many
clinicians recommend the continued
use of prenatal vitamin supplements
during lactation.109
The mothers diet should include an
average daily intake of 200 to 300 mg
of the -3 long-chain polyunsaturated
fatty acids (docosahexaenoic acid
[DHA]) to guarantee a sufcient concentration of preformed DHA in the
milk.111,112 Consumption of 1 to 2 portions of sh (eg, herring, canned light

tuna, salmon) per week will meet
this need. The concern regarding the
possible risk from intake of excessive
mercury or other contaminants is
offset by the neurobehavioral benets
of an adequate DHA intake and can be
minimized by avoiding the intake of
predatory sh (eg, pike, marlin, mackerel, tile sh, swordsh).113 Poorly
nourished mothers or those on selective vegan diets may require a supplement of DHA as well as multivitamins.
MATERNAL MEDICATIONS
Recommendations regarding breastfeeding in situations in which the
mother is undergoing either diagnostic
procedures or pharmacologic therapy
must balance the benets to the infant
and the mother against the potential
risk of drug exposure to the infant.
There are only a limited number of
agents that are contraindicated, and
an appropriate substitute usually can
be found. The most comprehensive, upto-date source of information regarding the safety of maternal medications
when the mother is breastfeeding is
LactMed, an Internet-accessed source
published by the National Library of
Medicine/National Institutes of Health.114
A forthcoming AAP policy statement
on the transfer of drugs and other
chemicals into human milk will provide additional recommendations, with
particular focus on psychotropic drugs,
herbal products, galactagogues, narcotics, and pain medications. 115 In
general, breastfeeding is not recommended when mothers are receiving
medication from the following classes
of drugs: amphetamines, chemotherapy agents, ergotamines, and statins.
There are a wide variety of maternally
administered psychotropic agents for
which there are inadequate pharmacologic data with regard to human
milk and/or nursing infants blood
e833
concentrations. In addition, data regarding the long-term neurobehavioral

effects from exposure to these agents
during the critical developmental period of early infancy are lacking. A
recent comprehensive review noted
that of the 96 psychotropic drugs
available, pharmacologic and clinical
information was only available for 62
(65%) of the drugs.116 In only 19 was
there adequate information to allow
for dening a safety protocol and thus
qualifying to be compatible for use by
lactating mothers. Among the agents
considered to be least problematic
were the tricyclic antidepressants amitriptyline and clomipramine and the
selective serotonin-reuptake inhibitors
paroxetine and sertraline.
Detailed guidelines regarding the necessity for and duration of temporary
cessation of breastfeeding after maternal exposure to diagnostic radioactive compounds are provided by the
US Nuclear Regulatory Commission
and in medical reviews.117119 Special
precaution should be followed in the
situation of breastfeeding infants with
glucose-6-phosphate-dehydrogenase
deciency. Fava beans, nitrofurantoin,
primaquine, and phenazopyridine should
be avoided by the mother to minimize
the risk of hemolysis in the infant.120
HOSPITAL ROUTINES
The Sections on Breastfeeding and
Perinatal Pediatrics have published
the Sample Hospital Breastfeeding
Policy that is available from the AAP
Safe and Healthy Beginnings Web site.3,5
This sample hospital policy is based
on the detailed recommendations of
the previous AAP policy statement
Breastfeeding and the Use of Human
Milk1 as well as the principles of the
1991 WHO/UNICEF publication Tens
Steps to Successful Breastfeeding
(Table 4)121 and provides a template for
developing a uniform hospital policy for
support of breastfeeding.122 In particular,
e834
emphasis is placed on the need to revise

or discontinue disruptive hospital
policies that interfere with early skinto-skin contact, that provide water,
glucose water, or commercial infant
formula without a medical indication,
that restrict the amount of time the
infant can be with the mother, that
limit feeding duration, or that provide
unlimited pacier use.
In 2009, the AAP endorsed the Ten Steps
program (see Table 4). Adherence to
these 10 steps has been demonstrated
to increase rates of breastfeeding initiation, duration, and exclusivity.122,123
Implementation of the following 5 postpartum hospital practices has been
demonstrated to increase breastfeeding
duration, irrespective of socioeconomic
status: breastfeeding in the rst hour
after birth, exclusive breastfeeding,
rooming-in, avoidance of paciers, and
receipt of telephone number for support after discharge from the hospital.124
The CDC National Survey of Maternity
Practices in Infant Nutrition and Care
has assessed the lactation practices in
more than 80% of US hospitals and
noted that the mean score for implementation of the Ten Steps was only
65%.34,125 Fifty-eight percent of hospitals erroneously advised mothers to
limit suckling at the breast to a specied length of time, and 41% of the
hospitals gave paciers to more than
some of their newbornsboth practices that have been documented
to lower breastfeeding rates and duration.126 The survey noted that in
30% of all birth centers, more than
half of all newborns received supplementation commercial infant formula,
a practice associated with shorter
duration of breastfeeding and less
exclusivity.34,125 As indicated in the
benets section, this early supplementation may affect morbidity outcomes in this population. The survey
also reported that 66% of hospitals
TABLE 4 WHO/UNICEF Ten Steps to

Successful Breastfeeding
1. Have a written breastfeeding policy that is
routinely communicated to all health care staff.
2. Train all health care staff in the skills necessary
to implement this policy.
3. Inform all pregnant women about the benets
and management of breastfeeding.
4. Help mothers initiate breastfeeding within the
rst hour of birth.
5. Show mothers how to breastfeed and how to
maintain lactation even if they are separated
from their infants.
6. Give newborn infants no food or drink other
than breast milk, unless medically indicated.
7. Practice rooming-in (allow mothers and infants
to remain together) 24 h a day.
8. Encourage breastfeeding on demand.
9. Give no articial nipples or paciers to
breastfeeding infants.a
10. Foster the establishment of breastfeeding
support groups and refer mothers to them on
discharge from hospital.
a
The AAP does not support a categorical ban on paciers

because of their role in SIDS risk reduction and their
analgesic benet during painful procedures when breastfeeding cannot provide the analgesia. Pacier use in the
hospital in the neonatal period should be limited to specic medical indications such as pain reduction and
calming in a drug-exposed infant, for example. Mothers
of healthy term breastfed infants should be instructed to
delay pacier use until breastfeeding is well-established,
usually about 3 to 4 wk after birth.
reported that they distributed to

breastfeeding mothers discharge packs
that contained commercial infant formula, a practice that has been documented to negatively affect exclusivity
and duration of breastfeeding.127 Few
birth centers have model hospital policies (14%) and support breastfeeding
mothers after hospital discharge (27%).
Only 37% of centers practice more
than 5 of the 10 Steps and only 3.5%
practice 9 to 10 Steps.34
There is, thus, a need for a major
conceptual change in the organization
of the hospital services for the mother
and infant dyad (Table 5). This requires that medical and nursing routines and practices adjust to the
principle that breastfeeding should
begin within the rst hour after birth
(even for Cesarean deliveries) and
that infants must be continuously accessible to the mother by rooming-in
arrangements that facilitate aroundthe-clock, on-demand feeding for the

healthy infant. Formal staff training
should not only focus on updating
knowledge and techniques for breastfeeding support but also should acknowledge the need to change attitudes
and eradicate unsubstantiated beliefs
about the supposed equivalency of
breastfeeding and commercial infant
formula feeding. Emphasis should be
placed on the numerous benets of
exclusive breastfeeding. The importance
of addressing the issue of the impact
of hospital practices and policies on
breastfeeding outcomes is highlighted
by the decision of The Joint Commission
to adopt the rate of exclusive breast
milk feeding as a Perinatal Care Core
Measure.127 As such, the rate of exclusive breastfeeding during the hospital
stay has been conrmed as a critical
variable when measuring the quality of
care provided by a medical facility.
Pacier Use
Given the documentation that early use
of paciers may be associated with
less successful breastfeeding, pacier
use in the neonatal period should be
limited to specic medical situations.128
These include uses for pain relief, as
a calming agent, or as part of structured program for enhancing oral
motor function. Because pacier use
has been associated with a reduction
in SIDS incidence, mothers of healthy
term infants should be instructed to
use paciers at infant nap or sleep
time after breastfeeding is well established, at approximately 3 to 4
weeks of age.129131
Vitamins and Mineral Supplements
Intramuscular vitamin K1 (phytonadione) at a dose of 0.5 to 1.0 mg
should routinely be administered to
all infants on the rst day to reduce
the risk of hemorrhagic disease of the
newborn.132 A delay of administration
until after the rst feeding at the

breast but not later than 6 hours of
age is recommended. A single oral
dose of vitamin K should not be used,
because the oral dose is variably
absorbed and does not provide adequate concentrations or stores for the
breastfed infant.132
Vitamin D deciency/insufciency and
rickets has increased in all infants as
a result of decreased sunlight exposure secondary to changes in lifestyle,
dress habits, and use of topical sunscreen preparations. To maintain an
adequate serum vitamin D concentration, all breastfed infants routinely
should receive an oral supplement of
vitamin D, 400 U per day, beginning at
hospital discharge.133
Supplementary uoride should not be
provided during the rst 6 months.
From age 6 months to 3 years, uoride
supplementation should be limited to
infants residing in communities where
the uoride concentration in the water
is <0.3 ppm.134 Complementary food
rich in iron and zinc should be introduced at about 6 months of age.
Supplementation of oral iron drops
before 6 months may be needed to
support iron stores.
Premature infants should receive
both a multivitamin preparation and
an oral iron supplement until they are
ingesting a completely mixed diet and
their growth and hematologic status
are normalized.
GROWTH
The growth pattern of healthy term
breastfed infants differs from the
existing CDC reference growth curves,
which are primarily based on data
from few breastfeeding infants. The
WHO multicenter curves are based on
combined longitudinal data from
healthy breastfed infants from birth
to 24 months and cross-sectional data
from 2 to 5 years of the same children
from 6 diverse geographical areas
TABLE 5 Recommendations on
Breastfeeding Management for
Healthy Term Infants
1. Exclusive breastfeeding for about 6 mo
Breastfeeding preferred; alternatively
expressed mothers milk, or donor milk
To continue for at least the rst year and
beyond for as long as mutually desired by
mother and child
Complementary foods rich in iron and other
micronutrients should be introduced at about 6
mo of age
2. Peripartum policies and practices that optimize
breastfeeding initiation and maintenance
should be compatible with the AAP and
Academy of Breastfeeding Medicine Model
Hospital Policy and include the following:
Direct skin-to-skin contact with mothers
immediately after delivery until the rst feeding
is accomplished and encouraged throughout
the postpartum period
Delay in routine procedures (weighing,
measuring, bathing, blood tests, vaccines, and
eye prophylaxis) until after the rst feeding is
completed
Delay in administration of intramuscular
vitamin K until after the rst feeding is
completed but within 6 h of birth
Ensure 8 to 12 feedings at the breast every
24 h
Ensure formal evaluation and documentation
of breastfeeding by trained caregivers
(including position, latch, milk transfer,
examination) at least for each nursing shift
Give no supplements (water, glucose water,
commercial infant formula, or other uids) to
breastfeeding newborn infants unless medically
indicated using standard evidence-based
guidelines for the management of
hyperbilirubinemia and hypoglycemia
Avoid routine pacier use in the postpartum
period
Begin daily oral vitamin D drops (400 IU) at
hospital discharge
3. All breastfeeding newborn infants should be
seen by a pediatrician at 3 to 5 d of age, which
is within 48 to 72 h after discharge from the
hospital
Evaluate hydration (elimination patterns)
Evaluate body wt gain (body wt loss no more
than 7%
from birth and no further wt loss by day 5:
assess feeding and consider more frequent
follow-up)
Discuss maternal/infant issues
Observe feeding
4. Mother and infant should sleep in proximity
to each other to facilitate breastfeeding
5. Pacier should be offered, while placing infant
in back-to-sleep-position, no earlier than 3 to
4 wk of age and after breastfeeding has been
established
e835
(Brazil, Ghana, India, Norway, Oman,

and the United States).135 As such, the
WHO curves are standards and are
the normative model for growth and
development irrespective of infant
ethnicity or geography reecting the
optimal growth of the breastfed infant.136 Use of the WHO curves for the
rst 2 years allows for more accurate
monitoring of weight and height for
age and, in comparison with use of
the CDC reference curves, results in
more accurate (lower) rates of undernutrition and short stature and
(higher) rates of overweight. Furthermore, birth to 6-month growth
charts are available where the curves
are magnied to permit monitoring of
weight trajectories. As such, the WHO
curves serve as the best guide for
assessing lactation performance because
they minimize mislabeling clinical situations as inadequate breastfeeding and
identify more accurately and promptly
overweight and obese infants. As of September 2010, the CDC, with the concurrence of the AAP, recommended the use
of the WHO curves for all children
younger than 24 months.137,138
ROLE OF THE PEDIATRICIAN

Pediatricians have a critical role in
their individual practices, communities, and society at large to serve as
advocates and supporters of successful breastfeeding (Table 6).139 Despite this critical role, studies have
demonstrated lack of preparation and
knowledge and declining attitudes
regarding the feasibility of breastfeeding.140 The AAP Web site141 provides a wealth of breastfeeding-related
material and resources to assist and
support pediatricians in their critical
role as advocates of infant well-being.
This includes the Safe and Healthy
Beginnings toolkit,5 which includes resources for physicians ofce for promotion of breastfeeding in a busy
pediatric practice setting, a pocket
e836
TABLE 6 Role of the Pediatrician

1. Promote breastfeeding as the norm for infant
feeding.
2. Become knowledgeable in the principles and
management of lactation and breastfeeding.
3. Develop skills necessary for assessing the
adequacy of breastfeeding.
4. Support training and education for medical
students, residents and postgraduate
physicians in breastfeeding and lactation.
5. Promote hospital policies that are compatible
with the AAP and Academy of Breastfeeding
Medicine Model Hospital Policy and the WHO/
UNICEF Ten Steps to
Successful Breastfeeding.
6. Collaborate with the obstetric community to
develop optimal breastfeeding support
programs.
7. Coordinate with community-based health care
professionals and certied breastfeeding
counselors to ensure uniform and
comprehensive breastfeeding support.
guide for coding to facilitate appropriate payment, suggested guidelines for

telephone triage of maternal breastfeeding concerns, and information
regarding employer support for
breastfeeding in the workplace.
Evidence-based protocols from organizations such as the Academy of
Breastfeeding Medicine provide detailed clinical guidance for management of specic issues, including the
recommendations for frequent and
unrestricted time for breastfeeding so
as to minimize hyperbilirubinemia
and hypoglycemia.4,142,143 The critical
role that pediatricians play is highlighted by the recommended health
supervision visit at 3 to 5 days of age,
which is within 48 to 72 hours after
discharge from the hospital, as well
as pediatricians support of practices
that avoid nonmedically indicated
supplementation with commercial infant formula.144
Pediatricians also should serve as
breastfeeding advocates and educators and not solely delegate this role
to staff or nonmedical/lay volunteers.
Communicating with families that
breastfeeding is a medical priority that
is enthusiastically recommended by
their personal pediatrician will build
support for mothers in the early weeks

postpartum. To assist in the education of future physicians, the AAP recommends using the evidence-based
Breastfeeding Residency Curriculum,4
which has been demonstrated to improve knowledge, condence, practice
patterns, and breastfeeding rates. The
pediatricians own ofce-based practice should serve as a model for how
to support breastfeeding in the workplace. The pediatrician should also take
the lead in encouraging the hospitals
with which he or she is afliated to
provide proper support and facilities
for their employees who choose to
continue to breastfeed.
BUSINESS CASE FOR

BREASTFEEDING
A mother/baby-friendly worksite provides benets to employers, including
a reduction in company health care
costs, lower employee absenteeism,
reduction in employee turnover, and
increased employee morale and productivity.145,146 The return on investment has been calculated that for
every $1 invested in creating and
supporting a lactation support program (including a designated pump
site that guarantees privacy, availability of refrigeration and a handwashing facility, and appropriate
mother break time) there is a $2 to $3
dollar return.147 The Maternal and
Child Health Bureau of the US Department of Health and Human Services, with support from the Ofce of
Womens Health, has created a program, The Business Case for Breastfeeding, that provides details of
economic benets to the employer
and toolkits for the creation of such
programs.148 The Patient Protection
and Affordable Care Act passed by
Congress in March 2010 mandates
that employers provide reasonable
break time for nursing mothers and
private non-bathroom areas to express
breast milk during their workday.149

The establishment of these initiatives
as the standard workplace environment will support mothers in their
goal of supplying only breast milk to
their infants beyond the immediate
postpartum period.
CONCLUSIONS
Research and practice in the 5 years
since publication of the last AAP policy
statement have reinforced the conclusion that breastfeeding and the use of
human milk confer unique nutritional
and nonnutritional benets to the infant
and the mother and, in turn, optimize

infant, child, and adult health as well as
child growth and development. Recently, published evidence-based studies have conrmed and quantitated the
risks of not breastfeeding. Thus, infant
feeding should not be considered as
a lifestyle choice but rather as a basic
health issue. As such, the pediatricians
role in advocating and supporting
proper breastfeeding practices is essential and vital for the achievement of
this preferred public health goal.35
Richard J. Schanler, MD
SECTION ON BREASTFEEDING
EXECUTIVE COMMITTEE, 20112012
Margreete Johnston, MD
Susan Landers, MD
Larry Noble, MD
Kinga Szucs, MD
Laura Viehmann, MD
PAST CONTRIBUTING EXECUTIVE

COMMITTEE MEMBERS
Lori Feldman-Winter, MD
Ruth Lawrence, MD
STAFF
LEAD AUTHORS
Arthur I. Eidelman, MD
Sunnah Kim, MS
Ngozi Onyema, MPH
REFERENCES
1. Gartner LM, Morton J, Lawrence RA, et al;
American Academy of Pediatrics Section
on Breastfeeding. Breastfeeding and the
use of human milk. Pediatrics. 2005;115
(2):496506
2. Schanler RJ, Dooley S, Gartner LM, Krebs NF,
Mass SB. Breastfeeding Handbook for
Physicians. Elk Grove Village, IL: American
Academy of Pediatrics; Washington, DC:
American College of Obstetricians and
Gynecologists; 2006
3. American Academy of Pediatrics Section on
Breastfeeding. Sample Hospital Breastfeeding Policy for Newborns. Elk Grove Village, IL:
American Academy of Pediatrics; 2008
4. Feldman-Winter L, Barone L, Milcarek B,
et al. Residency curriculum improves
breastfeeding care. Pediatrics. 2010;126
(2):289297
5. American Academy of Pediatrics. Safe and
Health Beginnings: A Resource Toolkit for
Hospitals and Physicians Ofces. Elk
Grove Village, IL: American Academy of
Pediatrics; 2008
6. Centers for Disease Control and Prevention. Breastfeeding Among U.S. Children Born 19992006, CDC National
Immunization Survey. Atlanta, GA: Centers
for Disease Control and Prevention; 2010
7. McDowell MM, Wang C-Y, KennedyStephenson J. Breastfeeding in the
United States: Findings from the National
Health and Nutrition Examination Surveys,
19992006. NCHS Data Briefs, no. 5.
Hyatsville, MD: National Center for Health
Statistics; 2008
8. 2007 CDC National Survey of Maternity
Practices in Infant Nutrition and Care.
9.
10.
11.
12.
13.
14.
15.
Atlanta, GA: Centers for Disease Control

and Prevention; 2009
Ofce of Disease Prevention and Health
Promotion; US Department of Health and
Human Services. Healthy People 2010. Available at: www.healthypeople.gov. Accessed
June 3, 2011
Centers for Disease Control and Prevention. Breastfeeding report card
United States, 2010. Available at: www.cdc.
gov/breastfeeding/data/reportcard.htm.
Accessed June 3, 2011
U.S. Department of Health and Human
Services. Maternal, infant, and child
health. Healthy People 2020; 2010. Available at: http://healthypeople.gov/2020/
topicsobjectives2020/overview.aspx?
topicid=26. Accessed December 12, 2011
Centers for Disease Control and Prevention. Racial and ethnic differences in
breastfeeding initiation and duration, by
state National Immunization Survey,
United States, 20042008. MMWR Morb
Mortal Wkly Rep. 2010;59(11):327334
Ip S, Chung M, Raman G, et al; Tufts-New
England Medical Center Evidence-based
Practice Center. Breastfeeding and maternal
and infant health outcomes in developed
countries. Evid Rep Technol Assess (Full
Rep). 2007;153(153):1186
Ip S, Chung M, Raman G, Trikalinos TA, Lau J.
A summary of the Agency for Healthcare
Research and Qualitys evidence report
on breastfeeding in developed countries.
Breastfeed Med. 2009;4(suppl 1):S17S30
Chantry CJ, Howard CR, Auinger P. Full
breastfeeding duration and associated
decrease in respiratory tract infection in
16.
17.
18.
19.
20.
21.
22.
US children. Pediatrics. 2006;117(2):425

432
Nishimura T, Suzue J, Kaji H. Breastfeeding
reduces the severity of respiratory syncytial virus infection among young infants:
a multi-center prospective study. Pediatr
Int. 2009;51(6):812816
Duijts L, Jaddoe VW, Hofman A, Moll HA.
Prolonged and exclusive breastfeeding
reduces the risk of infectious diseases in
infancy. Pediatrics. 2010;126(1). Available
at: www.pediatrics.org/cgi/content/full/
126/1/e18
Quigley MA, Kelly YJ, Sacker A. Breastfeeding and hospitalization for diarrheal
and respiratory infection in the United
Kingdom Millennium Cohort Study. Pediatrics. 2007;119(4). Available at: www.
pediatrics.org/cgi/content/full/119/4/e837
Sullivan S, Schanler RJ, Kim JH, et al. An
exclusively human milk-based diet is associated with a lower rate of necrotizing
enterocolitis than a diet of human milk
and bovine milk-based products. J Pediatr.
2010;156(4):562567, e1
Hauck FR, Thompson JMD, Tanabe KO,
Moon RY, Vennemann MM. Breastfeeding
and reduced risk of sudden infant death
syndrome: a meta-analysis. Pediatrics.
2011;128(1):18
Chen A, Rogan WJ. Breastfeeding and the
risk of postneonatal death in the United
States. Pediatrics. 2004;113(5). Available
at: www.pediatrics.org/cgi/content/full/
113/5/e435
Task Force on Sudden Infant Death Syndrome. SIDS and other sleep-related infant
deaths: expansion of recommendations for
e837
23.
24.
25.
26.
27.
28.
29.
30.
31.
32.
e838
a safe infant sleeping environment. Pediatrics. 2011;128(5):10301039

Vennemann MM, Bajanowski T, Brinkmann B,
et al; GeSID Study Group. Does breastfeeding
reduce the risk of sudden infant death
syndrome? Pediatrics. 2009;123(3). Available at: www.pediatrics.org/cgi/content/
full/123/3/e406
Bartick M, Reinhold A. The burden of suboptimal breastfeeding in the United States:
a pediatric cost analysis. Pediatrics. 2010;
125(5). Available at: www.pediatrics.org/
cgi/content/full/125/5/e1048
Jones G, Steketee RW, Black RE, Bhutta ZA,
Morris SS; Bellagio Child Survival Study
Group. How many child deaths can we prevent this year? Lancet. 2003;362(9377):6571
Greer FR, Sicherer SH, Burks AW; American Academy of Pediatrics Committee on
Nutrition; ; American Academy of Pediatrics Section on Allergy and Immunology.
Effects of early nutritional interventions
on the development of atopic disease in
infants and children: the role of maternal
dietary restriction, breastfeeding, timing
of introduction of complementary foods,
and hydrolyzed formulas. Pediatrics. 2008;
121(1):183191
Zutavern A, Brockow I, Schaaf B, et al; LISA
Study Group. Timing of solid food introduction in relation to atopic dermatitis
and atopic sensitization: results from
a prospective birth cohort study. Pediatrics. 2006;117(2):401411
Poole JA, Barriga K, Leung DYM, et al.
Timing of initial exposure to cereal grains
and the risk of wheat allergy. Pediatrics.
2006;117(6):21752182
Zutavern A, Brockow I, Schaaf B, et al; LISA
Study Group. Timing of solid food introduction in relation to eczema, asthma,
allergic rhinitis, and food and inhalant
sensitization at the age of 6 years: results
from the prospective birth cohort study
LISA. Pediatrics. 2008;121(1). Available at:
www.pediatrics.org/cgi/content/full/121/
1/e44
Nwaru BI, Erkkola M, Ahonen S, et al. Age
at the introduction of solid foods during
the rst year and allergic sensitization at
age 5 years. Pediatrics. 2010;125(1):5059
Akobeng AK, Ramanan AV, Buchan I, Heller RF.
Effect of breast feeding on risk of coeliac
disease: a systematic review and metaanalysis of observational studies. Arch
Dis Child. 2006;91(1):3943
Barclay AR, Russell RK, Wilson ML, Gilmour WH,
Satsangi J, Wilson DC. Systematic review: the
role of breastfeeding in the development
of pediatric inammatory bowel disease.
J Pediatr. 2009;155(3):421426
33. Penders J, Thijs C, Vink C, et al. Factors

inuencing the composition of the intestinal microbiota in early infancy. Pediatrics. 2006;118(2):511521
34. Perrine CG, Shealy KM, Scanlon KS, et al;
Centers for Disease Control and Prevention (CDC). Vital signs: hospital practices to support breastfeedingUnited
States, 2007 and 2009. MMWR Morb Mortal Wkly Rep. 2011;60(30):10201025
35. U.S.Department of Health and Human Services, The Surgeon Generals Call to Action to
Support Breastfeeding. Available at: www.
surgeongeneral.gov/topics/breastfeeding/
Accessed March 28, 2011
36. Owen CG, Martin RM, Whincup PH, Smith GD,
Cook DG. Effect of infant feeding on the
risk of obesity across the life course:
a quantitative review of published evidence. Pediatrics. 2005;115(5):13671377
37. Parikh NI, Hwang SJ, Ingelsson E, et al.
Breastfeeding in infancy and adult cardiovascular disease risk factors. Am J Med.
2009;122(7):656663, e1
38. Metzger MW, McDade TW. Breastfeeding
as obesity prevention in the United States:
a sibling difference model. Am J Hum Biol.
2010;22(3):291296
39. Dewey KG, Lnnerdal B. Infant self-regulation
of breast milk intake. Acta Paediatr Scand.
1986;75(6):893898
40. Li R, Fein SB, Grummer-Strawn LM. Association of breastfeeding intensity and
bottle-emptying behaviors at early infancy
with infants risk for excess weight at late
infancy. Pediatrics. 2008;122(suppl 2):
S77S84
41. Li R, Fein SB, Grummer-Strawn LM. Do
infants fed from bottles lack self-regulation
of milk intake compared with directly
breastfed infants? Pediatrics. 2010;125(6).
Available at: www.pediatrics.org/cgi/
content/full/125/6/e1386
42. Rosenbauer J, Herzig P, Giani G. Early infant feeding and risk of type 1 diabetes
mellitusa nationwide population-based
case-control study in pre-school children.
Diabetes Metab Res Rev. 2008;24(3):211
222
43. Das UN. Breastfeeding prevents type 2
diabetes mellitus: but, how and why? Am J
Clin Nutr. 2007;85(5):14361437
44. Bener A, Hoffmann GF, Afy Z, Rasul K,
Tewk I. Does prolonged breastfeeding
reduce the risk for childhood leukemia
and lymphomas? Minerva Pediatr. 2008;60
(2):155161
45. Rudant J, Orsi L, Menegaux F, et al.
Childhood acute leukemia, early common
infections, and allergy: The ESCALE Study.
Am J Epidemiol. 2010;172(9):10151027
46. Kwan ML, Bufer PA, Abrams B, Kiley VA.

Breastfeeding and the risk of childhood
leukemia: a meta-analysis. Public Health
Rep. 2004;119(6):521535
47. Der G, Batty GD, Deary IJ. Effect of breast
feeding on intelligence in children: prospective study, sibling pairs analysis, and
meta-analysis. BMJ. 2006;333(7575):945
950
48. Kramer MS, Fombonne E, Igumnov S, et al;
Promotion of Breastfeeding Intervention
Trial (PROBIT) Study Group. Effects of
prolonged and exclusive breastfeeding on
child behavior and maternal adjustment:
evidence from a large, randomized trial.
Pediatrics. 2008;121(3). Available at: www.
49. Kramer MS, Aboud F, Mironova E, et al;
Promotion of Breastfeeding Intervention
Trial (PROBIT) Study Group. Breastfeeding
and child cognitive development: new evidence from a large randomized trial.
Arch Gen Psychiatry. 2008;65(5):578584
50. Kramer MS, Chalmers B, Hodnett ED,
et al; PROBIT Study Group (Promotion of
Breastfeeding Intervention Trial). Promotion of Breastfeeding Intervention Trial
(PROBIT): a randomized trial in the Republic of Belarus. JAMA. 2001;285(4):413
420
51. Vohr BR, Poindexter BB, Dusick AM, et al;
NICHD Neonatal Research Network. Benecial effects of breast milk in the neonatal
intensive care unit on the developmental
outcome of extremely low birth weight
infants at 18 months of age. Pediatrics.
2006;118(1). Available at: www.pediatrics.
org/cgi/content/full/118/1/e115
52. Vohr BR, Poindexter BB, Dusick AM, et al;
National Institute of Child Health and Human Development National Research Network. Persistent benecial effects of
breast milk ingested in the neonatal intensive care unit on outcomes of extremely low birth weight infants at 30
months of age. Pediatrics. 2007;120(4).
Available at: www.pediatrics.org/cgi/
content/full/120/4/e953
53. Lucas A, Morley R, Cole TJ. Randomised
trial of early diet in preterm babies and
later intelligence quotient. BMJ. 1998;317
(7171):14811487
54. Isaacs EB, Fischl BR, Quinn BT, Chong WK,
Gadian DG, Lucas A. Impact of breast milk
on intelligence quotient, brain size, and
white matter development. Pediatr Res.
2010;67(4):357362
55. Furman L, Taylor G, Minich N, Hack M. The
effect of maternal milk on neonatal morbidity of very low-birth-weight infants. Arch
Pediatr Adolesc Med. 2003;157(1):6671
56. Lucas A, Cole TJ. Breast milk and neonatal

necrotising enterocolitis. Lancet. 1990;336
(8730):15191523
57. Sisk PM, Lovelady CA, Dillard RG, Gruber KJ,
OShea TM. Early human milk feeding
is associated with a lower risk of necrotizing enterocolitis in very low birth
weight infants. J Perinatol. 2007;27(7):
428433
58. Meinzen-Derr J, Poindexter B, Wrage L,
Morrow AL, Stoll B, Donovan EF. Role of
human milk in extremely low birth weight
infants risk of necrotizing enterocolitis or
death. J Perinatol. 2009;29(1):5762
59. Schanler RJ, Shulman RJ, Lau C. Feeding
strategies for premature infants: benecial outcomes of feeding fortied human
milk versus preterm formula. Pediatrics.
1999;103(6 pt 1):11501157
60. Hintz SR, Kendrick DE, Stoll BJ, et al; NICHD
Neonatal Research Network. Neurodevelopmental and growth outcomes of
extremely low birth weight infants after
necrotizing enterocolitis. Pediatrics. 2005;
115(3):696703
61. Shah DK, Doyle LW, Anderson PJ, et al.
Adverse neurodevelopment in preterm
infants with postnatal sepsis or necrotizing enterocolitis is mediated by white
matter abnormalities on magnetic resonance imaging at term. J Pediatr. 2008;
153(2):170175, e1
62. Hylander MA, Strobino DM, Dhanireddy R.
Human milk feedings and infection among
very low birth weight infants. Pediatrics.
63. Okamoto T, Shirai M, Kokubo M, et al.
Human milk reduces the risk of retinal
detachment in extremely low-birthweight
infants. Pediatr Int. 2007;49(6):894897
64. Lucas A. Long-term programming effects
of early nutritionimplications for the
preterm infant. J Perinatol. 2005;25(suppl
2):S2S6
65. Singhal A, Cole TJ, Lucas A. Early nutrition
in preterm infants and later blood pressure: two cohorts after randomised trials.
Lancet. 2001;357(9254):413419
66. Quigley MA, Henderson G, Anthony MY,
McGuire W. Formula milk versus donor
breast milk for feeding preterm or low
birth weight infants. Cochrane Database
Syst Rev. 2007;(4):CD002971
67. Slutzah M, Codipilly CN, Potak D, Clark RM,
Schanler RJ. Refrigerator storage of
expressed human milk in the neonatal
intensive care unit. J Pediatr. 2010;156(1):
2628
68. Henderson JJ, Evans SF, Straton JA, Priest SR,
Hagan R. Impact of postnatal depression
69.
70.
71.
72.
73.
74.
75.
76.
77.
78.
79.
80.
on breastfeeding duration. Birth. 2003;30

(3):175180
Strathearn L, Mamun AA, Najman JM,
OCallaghan MJ. Does breastfeeding protect against substantiated child abuse
and neglect? A 15-year cohort study. Pediatrics. 2009;123(2):483493
Krause KM, Lovelady CA, Peterson BL,
Chowdhury N, stbye T. Effect of breastfeeding on weight retention at 3 and 6
months postpartum: data from the North
Carolina WIC Programme. Public Health
Nutr. 2010;13(12):20192026
Stuebe AM, Rich-Edwards JW, Willett WC,
Manson JE, Michels KB. Duration of lactation and incidence of type 2 diabetes.
JAMA. 2005;294(20):26012610
Schwarz EB, Brown JS, Creasman JM,
et al. Lactation and maternal risk of type 2
diabetes: a population-based study. Am J
Med. 2010;123(9):863.e1.e6
Karlson EW, Mandl LA, Hankinson SE,
Grodstein F. Do breast-feeding and other
reproductive factors inuence future risk
of rheumatoid arthritis? Results from the
Nurses Health Study. Arthritis Rheum.
2004;50(11):34583467
Schwarz EB, Ray RM, Stuebe AM, et al.
Duration of lactation and risk factors for
maternal cardiovascular disease. Obstet
Gynecol. 2009;113(5):974982
Stuebe AM, Willett WC, Xue F, Michels
KB. Lactation and incidence of premenopausal breast cancer: a longitudinal study. Arch Intern Med. 2009;169(15):
13641371
Collaborative Group on Hormonal Factors
in Breast Cancer. Breast cancer and
breastfeeding: collaborative reanalysis of
individual data from 47 epidemiological
studies in 30 countries, including 50302
women with breast cancer and 96973
women without the disease. Lancet. 2002;
360(9328):187195
Lipworth L, Bailey LR, Trichopoulos D.
History of breast-feeding in relation to
breast cancer risk: a review of the epidemiologic literature. J Natl Cancer Inst.
2000;92(4):302312
World Health Organization. The optimal
duration of exclusive breastfeeding: report of an expert consultation. Available
at: hwww.who.int/nutrition/publications/
optimal_duration_of_exc_bfeeding_report_
eng.pdf. Accessed December 12, 2011
Institute of Medicine. Early childhood obesity
prevention policies. June 23, 2011. Available at: www.iom.edu/obesityyoungchildren.
Accessed December 12, 2011
Kramer MS, Kakuma R. Optimal duration
of exclusive breastfeeding [review]. The
81.
82.
83.
84.
85.
86.
87.
88.
89.
90.
Cochrane Library. January 21, 2009.

Available at: http://onlinelibrary.wiley.
com/doi/10.1002/14651858.CD003517/full.
Accessed December 12, 2011
Peterson AE, Perez-Escamilla R, Labbok MH,
Hight V, von Hertzen H, Van Look P. Multicenter study of the lactational amenorrhea
method (LAM) III: effectiveness, duration,
and satisfaction with reduced clientprovider contact. Contraception. 2000;62
(5):221230
Agostoni C, Decsi T, Fewtrell M, et al;
ESPGHAN Committee on Nutrition. Complementary feeding: a commentary by the
ESPGHAN Committee on Nutrition. J Pediatr
Gastroenterol Nutr. 2008;46(1):99110
Cattaneo A, Williams C, Palls-Alonso CR,
et al. ESPGHANs 2008 recommendation for
early introduction of complementary foods:
how good is the evidence? Matern Child
Nutr. 2011;7(4):335343
Gonalves DU, Proietti FA, Ribas JG, et al.
Epidemiology, treatment, and prevention
of human T-cell leukemia virus type 1associated diseases. Clin Microbiol Rev.
2010;23(3):577589
Arroyo Carrera I, Lpez Rodrguez MJ,
Sapia AM, Lpez Lafuente A, Sacristn AR.
Probable transmission of brucellosis by
breast milk. J Trop Pediatr. 2006;52(5):
380381
American Academy of Pediatrics. Tuberculosis. In: Pickering LK, Baker CJ, Kimberlin DW, Long SS, eds. Red Book: 2009
Report of the Committee on Infectious
Diseases. 28th ed. Elk Grove Village, IL:
American Academy of Pediatrics; 2009:
680-701
American Academy of Pediatrics. Varicella-zoster infections. In: Pickering LK,
Baker CJ, Kimberlin DW, Long SS, eds. Red
Book: 2009 Report of the Committee on
Infectious Diseases. 28th ed. Elk Grove
Village, IL: American Academy of Pediatrics; 2009:714-727
Centers for Disease Control and Prevention. 2009 H1N1 Flu (Swine Flu) and Feeding your Baby: What Parents Should Know.
Available at: http://www.cdc.gov/h1n1u/
infantfeeding.htm?s_cid=h1n1Flu_outbreak_
155. Accessed January 22, 2010
Horvath T, Madi BC, Iuppa IM, Kennedy GE,
Rutherford G, Read JS. Interventions for
preventing late postnatal mother-to-child
transmission of HIV. Cochrane Database
Syst Rev. 2009;21(1):CD006734
Chasela CS, Hudgens MG, Jamieson DJ,
et al; BAN Study Group. Maternal or infant antiretroviral drugs to reduce HIV-1
transmission. N Engl J Med. 2010;362(24):
22712281
e839
91. Shapiro RL, Hughes MD, Ogwu A, et al.

Antiretroviral regimens in pregnancy and
breast-feeding in Botswana. N Engl J Med.
2010;362(24):22822294
92. Hamele M, Flanagan R, Loomis CA, Stevens T,
Fairchok MP. Severe morbidity and mortality with breast milk associated cytomegalovirus infection. Pediatr Infect Dis J. 2010;
29(1):8486
93. Kurath S, Halwachs-Baumann G, Mller W,
Resch B. Transmission of cytomegalovirus
via breast milk to the prematurely born
infant: a systematic review. Clin Microbiol
Infect. 2010;16(8):11721178
94. Maschmann J, Hamprecht K, Weissbrich B,
Dietz K, Jahn G, Speer CP. Freeze-thawing of
breast milk does not prevent cytomegalovirus transmission to a preterm infant.
Arch Dis Child Fetal Neonatal Ed. 2006;91
(4):F288F290
95. Hamprecht K, Maschmann J, Mller D,
et al. Cytomegalovirus (CMV) inactivation
in breast milk: reassessment of pasteurization and freeze-thawing. Pediatr Res.
2004;56(4):529535
96. Jansson LM; Academy of Breastfeeding
Medicine Protocol Committee. ABM clinical protocol #21: Guidelines for breastfeeding and the drug-dependent woman.
Breastfeed Med. 2009;4(4):225228
97. Garry A, Rigourd V, Amirouche A, Fauroux V,
Aubry S, Serreau R. Cannabis and breastfeeding. J Toxicol. 2009;2009:596149
98. Little RE, Anderson KW, Ervin CH, Worthington-Roberts B, Clarren SK. Maternal
alcohol use during breast-feeding and infant mental and motor development at one
year. N Engl J Med. 1989;321(7):425430
99. Mennella JA, Pepino MY. Breastfeeding
and prolactin levels in lactating women
with a family history of alcoholism. Pediatrics. 2010;125(5). Available at: www.pediatrics.
100. Subcommittee on Nutrition During Lactation, Institute of Medicine, National Academy of Sciences. Nutrition During Lactation.
Washington, DC: National Academies Press;
1991:113152
101. Koren G. Drinking alcohol while breastfeeding. Will it harm my baby? Can Fam
Physician. 2002;48:3941
102. Guedes HT, Souza LS. Exposure to maternal smoking in the rst year of life
interferes in breast-feeding protective effect against the onset of respiratory allergy from birth to 5 yr. Pediatr Allergy
Immunol. 2009;20(1):3034
103. Liebrechts-Akkerman G, Lao O, Liu F, et al.
Postnatal parental smoking: an important
risk factor for SIDS. Eur J Pediatr. 2011;
170(10):12811291
e840
104. Yilmaz G, Hizli S, Karacan C, Yurdakk K,

Coskun T, Dilmen U. Effect of passive
smoking on growth and infection rates of
breast-fed and non-breast-fed infants.
Pediatr Int. 2009;51(3):352358
105. Vio F, Salazar G, Infante C. Smoking during
pregnancy and lactation and its effects on
breast-milk volume. Am J Clin Nutr. 1991;
54(6):10111016
106. Hopkinson JM, Schanler RJ, Fraley JK,
Garza C. Milk production by mothers of
premature infants: inuence of cigarette
smoking. Pediatrics. 1992;90(6):934938
107. Butte NF. Maternal nutrition during lactation. Pediatric Up-to-Date. 2010. Available at:
http://www.uptodate.com/contents/maternalnutrition-during-lactation?source=search_
result&search=maternal+nutrition&
selectedTitle=2%7E150. Accessed October
29, 2010
108. Zeisel SH. Is maternal diet supplementation benecial? Optimal development of
infant depends on mothers diet. Am J Clin
Nutr. 2009;89(2):685S687S
109. Picciano MF, McGuire MK. Use of dietary
supplements by pregnant and lactating
women in North America. Am J Clin Nutr.
2009;89(2):663S667S
110. Whitelaw A. Historical perspectives: perinatal proles: Robert McCance and Elsie
Widdowson: pioneers in neonatal science.
NeoReviews. 2007;8(11):e455e458
111. Simopoulos AP, Leaf A, Salem N Jr. Workshop on the essentiality of and recommended dietary intakes for omega-6 and
omega-3 fatty acids. J Am Coll Nutr. 1999;
18(5):487489
112. Carlson SE. Docosahexaenoic acid supplementation in pregnancy and lactation.
Am J Clin Nutr. 2009;89(2):678S684S
113. Koletzko B, Cetin I, Brenna JT; Perinatal
Lipid Intake Working Group; ; Child Health
Foundation; ; Diabetic Pregnancy Study
Group; ; European Association of Perinatal
Medicine; ; European Association of Perinatal Medicine; ; European Society for
Clinical Nutrition and Metabolism; ; European Society for Paediatric Gastroenterology, Hepatology and Nutrition, Committee
on Nutrition; ; International Federation of
Placenta Associations; ; International Society for the Study of Fatty Acids and Lipids.
Dietary fat intakes for pregnant and lactating women. Br J Nutr. 2007;98(5):873
877
114. Drugs and Lactation Database. 2010. Available at: http://toxnet.nlm.nih.gov/cgi-bin/
sis/htmlgen?LACT. Accessed September 17,
2009
115. Committee on Drugs, American Academy
of Pediatrics. The transfer of drugs and
116.
117.
118.
119.
120.
121.
122.
123.
124.
125.
126.
127.
128.
other chemicals into human milk. Pediatrics. 2011, In press

Fortinguerra F, Clavenna A, Bonati M.
Psychotropic drug use during breastfeeding: a review of the evidence. Pediatrics. 2009;124(4). Available at: www.
US Nuclear Regulatory Commission. Control of access to high and very high radiation areas in nuclear power plants.
USNRC Regulatory Guide 8.38. June 1993.
Available at: www.nrc.gov/reading-rm/
doc-collections/reg-guides/occupationalhealth/rg/8-38/08-038.pdf.
International Commission on Radiological
Protection. Doses to infants from ingestion
of radionuclides in mothers milk. ICRP
Publication 95. Ann ICRP. 2004;34(34):1-27
Stabin MG, Breitz HB. Breast milk excretion of radiopharmaceuticals: mechanisms, ndings, and radiation dosimetry. J
Nucl Med. 2000;41(5):863873
Kaplan M, Hammerman C. Severe neonatal
hyperbilirubinemia. A potential complication
of glucose-6-phosphate dehydrogenase deciency. Clin Perinatol. 1998;25(3):575590,
viii
World Health Organization. Evidence for
the Ten Steps to Successful Breastfeeding.
Geneva, Switzerland: World Health Organization; 1998
World Health Organization; United Nations
Childrens Fund. Protecting, Promoting,
and Supporting Breastfeeding: The Special
Role of Maternity Services. Geneva, Switzerland: World Health Organization; 1989
Philipp BL, Merewood A, Miller LW, et al.
Baby-friendly hospital initiative improves
breastfeeding initiation rates in a US hospital setting. Pediatrics. 2001;108(3):677681
Murray EK, Ricketts S, Dellaport J. Hospital
practices that increase breastfeeding duration: results from a population-based
study. Birth. 2007;34(3):202211
Centers for Disease Control and Prevention. Breastfeeding-related maternity
practices at hospitals and birth centers
United States, 2007. MMWR Morb Mortal
Wkly Rep. 2008;57(23):621625
Dewey KG, Nommsen-Rivers LA, Heinig MJ,
Cohen RJ. Risk factors for suboptimal infant breastfeeding behavior, delayed onset
of lactation, and excess neonatal weight
loss. Pediatrics. 2003;112(3 pt 1):607619
The Joint Commission: Specications Manual for Joint Commission National Quality
Core Measures. Available at: http://manual.
jointcommission.org/releases/TJC2011A/.
Accessed January 12, 2011
OConnor NR, Tanabe KO, Siadaty MS,
Hauck FR. Paciers and breastfeeding:
129.
130.
131.
132.
133.
134.
135.
a systematic review. Arch Pediatr Adolesc

Med. 2009;163(4):378382
Hauck FR, Omojokun OO, Siadaty MS. Do
paciers reduce the risk of sudden infant
death syndrome? A meta-analysis. Pediatrics.
American Academy of Pediatrics Task
Force on Sudden Infant Death Syndrome.
The changing concept of sudden infant
death syndrome: diagnostic coding shifts,
controversies regarding the sleeping environment, and new variables to consider
in reducing risk. Pediatrics. 2005;116(5):
12451255
Li DK, Willinger M, Petitti DB, Odouli R, Liu L,
Hoffman HJ. Use of a dummy (pacier)
during sleep and risk of sudden infant death
syndrome (SIDS): population based casecontrol study. BMJ. 2006;332(7532):1822
American Academy of Pediatrics Committee on Fetus and Newborn. Controversies
concerning vitamin K and the newborn.
Pediatrics. 2003;112(1 pt 1):191192
Wagner CL, Greer FR; American Academy
of Pediatrics Section on Breastfeeding; ;
American Academy of Pediatrics Committee on Nutrition. Prevention of rickets and
vitamin D deciency in infants, children,
and adolescents. Pediatrics. 2008;122(5):
11421152
American Academy of Pediatric Dentistry.
Guidelines for Fluoride Therapy, Revised
2000. Available at: http://www.aapd.org/pdf/
uoridetherapy.pdf. Accessed September 17,
2009
Garza C, de Onis M. Rationale for developing a new international growth
136.
137.
138.
139.
140.
141.
142.
143.
reference. Food Nutr Bull. 2004;25(suppl

1):S5S14
de Onis M, Garza C, Onyango AW, Borghi E.
Comparison of the WHO child growth
standards and the CDC 2000 growth
charts. J Nutr. 2007;137(1):144148
Grummer-Strawn LM, Reinold C, Krebs NF;
Centers for Disease Control and Prevention. Use of World Health Organization
and CDC growth charts for children aged
059 months in the United States. MMWR
Recomm Rep. 2010;59(RR-9):115
Grummer-Strawn LM, Reinold C, Krebs
NFCenters for Disease Control and Prevention. Use of World Health Organization
and CDC growth charts for children aged
0-59 months in the United States. MMWR
Recomm Rep. 2010;59(RR-9):115
Schanler RJ. The pediatrician supports
breastfeeding. Breastfeed Med. 2010;5(5):
235236
Feldman-Winter LB, Schanler RJ, OConnor KG,
Lawrence RA. Pediatricians and the promotion and support of breastfeeding. Arch
Pediatr Adolesc Med. 2008;162(12):1142
1149
American Academy of Pediatrics. American Academy of Pediatrics Breastfeeding
Initiatives. 2010. Available at: http://www.
aap.org/breastfeeding. Accessed September 17, 2009
Academy of Breastfeeding Medicine Protocol Committee. Clinical Protocols. Available at http://www.bfmed.org/Resources/
Protocols.aspx. Accessed January 22, 2010
American Academy of Pediatrics Subcommittee on Hyperbilirubinemia. Management
of hyperbilirubinemia in the newborn
144.
145.
146.
147.
148.
149.
150.
151.
infant 35 or more weeks of gestation.

Pediatrics. 2004;114(1):297316
American Academy of Pediatrics, Committee on Practice and Ambulatory Medicine
and Bright Futures Steering Committee.
Recommendations for preventive pediatric
health care. Pediatrics. 2007;120(6):1376
Cohen R, Mrtek MB, Mrtek RG. Comparison
of maternal absenteeism and infant illness
rates among breast-feeding and formulafeeding women in two corporations. Am J
Health Promot. 1995;10(2):148153
Ortiz J, McGilligan K, Kelly P. Duration of
breast milk expression among working
mothers enrolled in an employer-sponsored
lactation program. Pediatr Nurs. 2004;30(2):
111119
Tuttle CR, Slavit WI. Establishing the business case for breastfeeding. Breastfeed
Med. 2009;4(suppl 1):S59S62
US Department of Health and Human
Services Ofce on Womens Health. Business
case for breast feeding. 2010. Available at:
www.womenshealth.gov/breastfeeding/
government-in-action/business-case-forbreastfeeding. Accessed September 24, 2010
Patient Protection and Affordable Care Act
2010, Public Law 111-148. Title IV, x4207,
USC HR 3590, (2010)
Hurst NM, Myatt A, Schanler RJ. Growth
and development of a hospital-based lactation program and mothers own milk
bank. J Obstet Gynecol Neonatal Nurs.
1998;27(5):503510
Schanler RJ, Fraley JK, Lau C, Hurst NM,
Horvath L, Rossmann SN. Breastmilk cultures
and infection in extremely premature
infants. J Perinatol. 2011;31(5):335338
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FROM THE AMERICAN ACADEMY OF PEDIATRICS

Organizational Principles to Guide and Dene the Child

Breastfeeding and the Use of Human Milk

PEDIATRICS Volume 129, Number 3, March 2012

of breastfeeding for 1 year or longer

TABLE 1 Healthy People Targets 2010 and

2007 data reported in 2011.10

FROM THE AMERICAN ACADEMY OF PEDIATRICS

with a higher income ineligible for

FROM THE AMERICAN ACADEMY OF PEDIATRICS

TABLE 2 Dose-Response Benets of Breastfeedinga

to 6 months had a fourfold increase

infants who exclusively breastfed for 6

Any breastfeeding compared with exclusive commercial infant formula

PEDIATRICS Volume 129, Number 3, March 2012

Gastrointestinal Tract Infections

Meta-analyses of 4 randomized clinical

reducing the incidence of clinical

FROM THE AMERICAN ACADEMY OF PEDIATRICS

susceptibility of the infant. Different

FROM THE AMERICAN ACADEMY OF PEDIATRICS

addition, higher intelligence scores

These neurodevelopmental outcomes

confounders, that the rate of abuse/

Cumulative lactation experience also

Compared with infants who never

FROM THE AMERICAN ACADEMY OF PEDIATRICS

The AAP is cognizant that for some

year and beyond as more and varied

FROM THE AMERICAN ACADEMY OF PEDIATRICS

from human milk. Infants in areas

milk, and their use by breastfeeding

milk.111,112 Consumption of 1 to 2 portions of sh (eg, herring, canned light

concentrations. In addition, data regarding the long-term neurobehavioral

FROM THE AMERICAN ACADEMY OF PEDIATRICS

emphasis is placed on the need to revise

TABLE 4 WHO/UNICEF Ten Steps to

The AAP does not support a categorical ban on paciers

reported that they distributed to

FROM THE AMERICAN ACADEMY OF PEDIATRICS

arrangements that facilitate aroundthe-clock, on-demand feeding for the

until after the rst feeding at the

(Brazil, Ghana, India, Norway, Oman,

ROLE OF THE PEDIATRICIAN

FROM THE AMERICAN ACADEMY OF PEDIATRICS

TABLE 6 Role of the Pediatrician

guide for coding to facilitate appropriate payment, suggested guidelines for

support for mothers in the early weeks

BUSINESS CASE FOR

FROM THE AMERICAN ACADEMY OF PEDIATRICS

breast milk during their workday.149

and the mother and, in turn, optimize

PAST CONTRIBUTING EXECUTIVE

PEDIATRICS Volume 129, Number 3, March 2012

Atlanta, GA: Centers for Disease Control

US children. Pediatrics. 2006;117(2):425

a safe infant sleeping environment. Pediatrics. 2011;128(5):10301039